Increased Frequency of Genomic Alterations in Staphylococcus aureus during Chronic Infection Is in Part Due to Phage Mobilization

We assessed the nature and frequency of genome alterations in Staphylococcus aureus during chronic lung infection in patients with cystic fibrosis (CF) and during colonization of the nares in healthy individuals. Only individuals harboring the same S. aureus clone on consecutive samplings were inclu...

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Bibliographic Details
Published in:The Journal of infectious diseases Vol. 189; no. 4; pp. 724 - 734
Main Authors: Goerke, Christiane, y Papenberg, Saskia Matias, Dasbach, Simone, Dietz, Klaus, Ziebach, Rita, Kahl, Barbara C., Wolz, Christiane
Format: Journal Article
Language:English
Published: Chicago, IL The University of Chicago Press 15-02-2004
University of Chicago Press
Oxford University Press
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Summary:We assessed the nature and frequency of genome alterations in Staphylococcus aureus during chronic lung infection in patients with cystic fibrosis (CF) and during colonization of the nares in healthy individuals. Only individuals harboring the same S. aureus clone on consecutive samplings were included in the present study. Clone definition was based on pulsed-field gel electrophoresis (PFGE) analysis. Minor fragment variations in consecutive clones were interpreted as genome alterations. The frequency of genome alterations was significantly higher in S. aureus derived from patients with CF (mean time, 1.03 years) than in isolates derived from healthy individuals (mean time, 13.4 years). In total, 19 S. aureus strain pairs showing genome alterations were available for molecular analysis to clarify the nature of recombinational events in the host environment. In 8 cases, genome alteration could be linked to phage mobilization. Phage conversion of β-toxin production was evident in 7 pairs. In 1 strain pair, changes in the PFGE pattern were accompanied by deletion of a phage similar to ETA. Obviously, phage mobilization plays an important role in vivo. During long-termlung infection in patients with CF, the specific host response and/or the regular exposure to antibiotics exercises strong selective pressure on the pathogen. Genome plasticity may facilitate the adaptation to various host conditions.
Bibliography:ark:/67375/HXZ-JTXXC3WN-X
Financial support: Deutsche Forschungsgemeinschaft (grants Wo 578/3-2 and Wo 578/3-3); Mukoviszidose e.V.
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ISSN:0022-1899
1537-6613
DOI:10.1086/381502